G Eisenhofer, HJ Timmers, JWM Lenders… - Journal of Clinical …, 2011 - Endocrine Soc ... Among patients without evidence of hereditarydisease, tumors showing both increased plasma concentrations of metanephrine (>61 pg/ml) and relative increases of metanephrine above the cut-off (>5%) were designated as those with appreciable epinephrine production (ie ... Cited by 2 - Related articles - All 3 versions
[PDF] from molmed.orgW Pavicic, E Perkiö, S Kaur… - … medicine (Cambridge, Mass …, 2011 - molmed.org ... gastric vs. endometrial), MMR-proficiency vs. deficiency, and sporadic vs. hereditary disease. In particular, ... status, and sporadic vs. hereditarydisease The 9 miRNA loci each of which showed a predominant pattern of alterations in Fig. ... Cited by 1 - Related articles - View as HTML - All 3 versions
[PDF] from mit.eduY Erlich, S Edvardson, E Hodges, S Zenvirt… - Genome …, 2011 - genome.cshlp.org Whole exome sequencing has become a pivotal methodology for rapid and cost-effective detection of pathogenic variations in Mendelian disorders. A major challenge of this approach is determining the causative mutation from a substantial number of bystander variations that do not play ... Cited by 5 - Related articles - All 8 versions
V Busskamp… - Current Opinion in Neurobiology, 2011 - Elsevier ... Available online 25 June 2011. Retinitis pigmentosa is a hereditary eye disease that affects photoreceptors and leads to blindness. The ... Retinitis pigmentosa is a hereditary disease of photoreceptors that causes blindness. ► The ... Related articles - All 2 versions
[PDF] from pjms.com.pkBA Dorum, I Silfeler, Y Canbak… - Pak J Med Sci April-June, 2011 - pjms.com.pk ... Muscular dystrophy is a rare hereditarydisease compared to other disease causing elevation of transaminase. ... Muscular dystro- phy is a group of hereditarydisease affecting many systems, as well as muscular and skeletal systems. ... Related articles - All 2 versions
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